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2020
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- Diastereoselective synthesis and structure–affinity relationships of σ
1 receptor ligands with spirocyclic scaffold. Tobias Winge, Dirk Schepmann, Judith Schmidt, Constantin Daniliuc, Ernst-Ulrich Würthwein, Bernhard Wünsch
, Org. Biomol. Chem.
, 2023
, 21
, 7730
- Regioselective synthesis of novel 2,3,4,4a-tetrahydro-1H-carbazoles and their cholinesterase inhibitory activities. Maria Aqeel Khan, Saba Fazal-ur-Rehman, Abdul Hameed, Shazia Kousar, Kourosh Dalvandi, Sammer Yousuf, Muhammad Iqbal Choudhary, Fatima Zehra Basha
, RSC Adv.
, 2015
, 5
, 59240
- History, biology and chemistry of Mycobacterium ulcerans infections (Buruli ulcer disease). Anne-Caroline Chany, Cédric Tresse, Virginie Casarotto, Nicolas Blanchard
, Nat. Prod. Rep.
, 2013
, 30
, 1527
- Design and sterospecific synthesis of modular ligands based upon cis-1,3-trans-5-substituted cyclohexanes. John Fielden, Joanna Sprott, Leroy Cronin
, New J. Chem.
, 2005
, 29
, 1152
- Synthesis of a 2-deoxyglucosyl analogue of medermycin. Margaret A. Brimble, Timothy J. Brenstrum
, J. Chem. Soc., Perkin Trans. 1
, 2001
, 1624
- Racemic N-aryl bis(amidines) and bis(amidinates): on the trail of enantioselective organolanthanide catalysts. Michael S. Hill, Peter B. Hitchcock, Stephen M. Mansell
, Dalton Trans.
, 2006
, 1544
- Synthesis, structure and reactions of the most twisted amide. Anthony J. Kirby, Igor V. Komarov, Neil Feeder
, J. Chem. Soc., Perkin Trans. 2
, 2001
, 522
- Synthesis of 3-azido-2,3,6-trideoxy-β-d-arabino-hexopyranosyl pyranonaphthoquinone analogues of medermycin. Margaret A. Brimble, Roger M. Davey, Malcolm D. McLeod, Maureen Murphy
, Org. Biomol. Chem.
, 2003
, 1
, 1690
- A comparison of non-covalent interactions in the crystal structures of two σ-alkane complexes of Rh exhibiting contrasting stabilities in the solid state. M. Arif Sajjad, Stuart A. Macgregor, Andrew S. Weller
, Faraday Discuss.
, 2023
, 244
, 222
- New insights into the catalytic reduction of aliphatic nitro compounds with hypophosphites under ultrasonic irradiation. S. Letort, M. Lejeune, N. Kardos, E. Métay, F. Popowycz, M. Lemaire, M. Draye
, Green Chem.
, 2017
, 19
, 4583